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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835854Generated: October 26, 2026

Spiro[indoline-3,3'-perhydroazepin]-2-one hydrochloride → Spiro[indoline-3,3'-perhydroazepin]-2-one

https://huagongshe.com/reaction/1835854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSpiro[indoline-3,3'-perhydroazepin]-2-one hydrochlorideHCID 23500654—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductSpiro[indoline-3,3'-perhydroazepin]-2-oneHCID 23500655—

Reaction Steps

Spiro[indoline-3,3′-perhydroazepin]-2-one hydrochloride. The compound from the previous step was hydrogenated in acetic acid over 10% Pd/C at 40 psi H, for 48 h. Evaporation and extractive work-up gave the title compound as a yellow solid (1.51 g). MS (TSP+) m/z: 217 (M+H+, 100) which was converted to the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774132B1
Source datasetuspto-grants-2004_08
ORD IDord-6486a40a7c8c450a86650e2eaed5f1d9
Source noteuspto-grants-2004_08